A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3637772



Internal ID6677873
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:6828112..6847227hg38UCSC Ensembl
chr16:6878113..6897228hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3819116
hg1919116
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15365724, essv15365725
SamplesHG02108, HG03237
Known GenesRBFOX1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3637772
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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